Hopp Children's Cancer Center Heidelberg (KiTZ), Im Neuenheimer Feld 430, 69120, Heidelberg, Germany.
Clinical Cooperation Unit Pediatric Oncology, German Cancer Research Center (DKFZ) and German Consortium for Translational Cancer Research (DKTK), Heidelberg, Germany.
J Neurooncol. 2023 Dec;165(3):467-478. doi: 10.1007/s11060-023-04500-6. Epub 2023 Nov 24.
Although pediatric low-grade gliomas (pLGG) are the most common pediatric brain tumors, patient-derived cell lines reflecting pLGG biology in culture are scarce. This also applies to the most common pLGG subtype pilocytic astrocytoma (PA). Conventional cell culture approaches adapted from higher-grade tumors fail in PA due to oncogene-induced senescence (OIS) driving tumor cells into arrest. Here, we describe a PA modeling workflow using the Simian Virus large T antigen (SV40-TAg) to circumvent OIS.
18 pLGG tissue samples (17 (94%) histological and/or molecular diagnosis PA) were mechanically dissociated. Tumor cell positive-selection using A2B5 was perfomed in 8/18 (44%) cases. All primary cell suspensions were seeded in Neural Stem Cell Medium (NSM) and Astrocyte Basal Medium (ABM). Resulting short-term cultures were infected with SV40-TAg lentivirus. Detection of tumor specific alterations (BRAF-duplication and BRAF V600E-mutation) by digital droplet PCR (ddPCR) at defined time points allowed for determination of tumor cell fraction (TCF) and evaluation of the workflow. DNA-methylation profiling and gene-panel sequencing were used for molecular profiling of primary samples.
Primary cell suspensions had a mean TCF of 55% (+/- 23% (SD)). No sample in NSM (0/18) and ten samples in ABM (10/18) were successfully transduced. Three of these ten (30%) converted into long-term pLGG cell lines (TCF 100%), while TCF declined to 0% (outgrowth of microenvironmental cells) in 7/10 (70%) cultures. Young patient age was associated with successful model establishment.
A subset of primary PA cultures can be converted into long-term cell lines using SV40-TAg depending on sample intrinsic (patient age) and extrinsic workflow-related (e.g. type of medium, successful transduction) parameters. Careful monitoring of sample-intrinsic and extrinsic factors optimizes the process.
尽管小儿低级别胶质瘤(pLGG)是最常见的小儿脑肿瘤,但在培养中反映 pLGG 生物学的患者源性细胞系却很少。这也适用于最常见的 pLGG 亚型毛细胞型星形细胞瘤(PA)。由于致癌基因诱导的衰老(OIS)使肿瘤细胞停滞,因此从高级别肿瘤中适应性修改的常规细胞培养方法在 PA 中失败。在这里,我们描述了一种使用猿猴病毒 40 型大 T 抗原(SV40-TAg)来规避 OIS 的 PA 建模工作流程。
对 18 个 pLGG 组织样本(17 个(94%)组织学和/或分子诊断为 PA)进行机械分离。在 8/18(44%)例中使用 A2B5 进行肿瘤细胞阳性选择。将所有原代细胞悬液接种于神经干细胞培养基(NSM)和星形胶质细胞基础培养基(ABM)中。用 SV40-TAg 慢病毒感染由此产生的短期培养物。通过数字液滴 PCR(ddPCR)在规定的时间点检测肿瘤特异性改变(BRAF 复制和 BRAF V600E 突变),可以确定肿瘤细胞分数(TCF)并评估该工作流程。使用 DNA 甲基化分析和基因面板测序对原代样本进行分子分析。
原代细胞悬液的平均 TCF 为 55%(+/-23%(SD))。在 NSM 中没有一个样本(0/18)和在 ABM 中有 10 个样本(10/18)成功转导。在这 10 个样本中,有 3 个(30%)转化为长期 pLGG 细胞系(TCF 为 100%),而在 7/10(70%)培养物中 TCF 下降到 0%(微环境细胞的生长)。年轻患者的年龄与成功建立模型有关。
根据样本内在(患者年龄)和外在工作流程相关(例如,培养基类型,成功转导)参数,使用 SV40-TAg 可以将一部分原代 PA 培养物转化为长期细胞系。仔细监测样本内在和外在因素可以优化该过程。